US7811498B2 - Process for the production of a shaped article - Google Patents
Process for the production of a shaped article Download PDFInfo
- Publication number
- US7811498B2 US7811498B2 US11/936,707 US93670707A US7811498B2 US 7811498 B2 US7811498 B2 US 7811498B2 US 93670707 A US93670707 A US 93670707A US 7811498 B2 US7811498 B2 US 7811498B2
- Authority
- US
- United States
- Prior art keywords
- solvent
- fiber layers
- shaped article
- fibers
- production
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related, expires
Links
- 238000000034 method Methods 0.000 title claims abstract description 45
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000002904 solvent Substances 0.000 claims abstract description 120
- 239000000835 fiber Substances 0.000 claims abstract description 94
- 229920000098 polyolefin Polymers 0.000 claims abstract description 36
- 230000006835 compression Effects 0.000 claims abstract description 18
- 238000007906 compression Methods 0.000 claims abstract description 18
- -1 polyethylene Polymers 0.000 claims description 23
- 239000004698 Polyethylene Substances 0.000 claims description 21
- 229920000573 polyethylene Polymers 0.000 claims description 21
- 239000012188 paraffin wax Substances 0.000 claims description 19
- 239000011159 matrix material Substances 0.000 claims description 10
- 238000010521 absorption reaction Methods 0.000 claims description 7
- 239000010410 layer Substances 0.000 description 34
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 12
- 230000008901 benefit Effects 0.000 description 10
- 239000002759 woven fabric Substances 0.000 description 9
- 239000002131 composite material Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 239000005662 Paraffin oil Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 239000012749 thinning agent Substances 0.000 description 3
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 208000002352 blister Diseases 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000001891 gel spinning Methods 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- 101000823778 Homo sapiens Y-box-binding protein 2 Proteins 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/28—Shaping operations therefor
- B29C70/40—Shaping or impregnating by compression not applied
- B29C70/42—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles
- B29C70/46—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles using matched moulds, e.g. for deforming sheet moulding compounds [SMC] or prepregs
- B29C70/465—Shaping or impregnating by compression not applied for producing articles of definite length, i.e. discrete articles using matched moulds, e.g. for deforming sheet moulding compounds [SMC] or prepregs and impregnating by melting a solid material, e.g. sheets, powders of fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/06—Fibrous reinforcements only
- B29C70/10—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres
- B29C70/16—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of substantial or continuous length
- B29C70/20—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of substantial or continuous length oriented in a single direction, e.g. roofing or other parallel fibres
- B29C70/202—Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres using fibres of substantial or continuous length oriented in a single direction, e.g. roofing or other parallel fibres arranged in parallel planes or structures of fibres crossing at substantial angles, e.g. cross-moulding compound [XMC]
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/04—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
- B29C70/28—Shaping operations therefor
- B29C70/30—Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core
- B29C70/34—Shaping by lay-up, i.e. applying fibres, tape or broadsheet on a mould, former or core; Shaping by spray-up, i.e. spraying of fibres on a mould, former or core and shaping or impregnating by compression, i.e. combined with compressing after the lay-up operation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2223/00—Use of polyalkenes or derivatives thereof as reinforcement
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/48—Wearing apparel
- B29L2031/4807—Headwear
- B29L2031/4814—Hats
- B29L2031/4821—Helmets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/911—Penetration resistant layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1362—Textile, fabric, cloth, or pile containing [e.g., web, net, woven, knitted, mesh, nonwoven, matted, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24058—Structurally defined web or sheet [e.g., overall dimension, etc.] including grain, strips, or filamentary elements in respective layers or components in angular relation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24058—Structurally defined web or sheet [e.g., overall dimension, etc.] including grain, strips, or filamentary elements in respective layers or components in angular relation
- Y10T428/24124—Fibers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/249933—Fiber embedded in or on the surface of a natural or synthetic rubber matrix
- Y10T428/249938—Composite or conjugate fiber [e.g., fiber contains more than one chemically different material in monofilament or multifilament form, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/643—Including parallel strand or fiber material within the nonwoven fabric
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/647—Including a foamed layer or component
- Y10T442/651—Plural fabric layers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/696—Including strand or fiber material which is stated to have specific attributes [e.g., heat or fire resistance, chemical or solvent resistance, high absorption for aqueous compositions, water solubility, heat shrinkability, etc.]
Definitions
- the invention relates to a process for the production of a shaped article comprising the compression of one or more fibre layers containing polyolefin fibres.
- the invention also relates to shaped articles obtainable with the process according to the invention and their use in anti-ballistic applications.
- SEA Specific Energy Absorption
- MSC AK-47 Mild Steel Core
- the fibre layers contain 0.02 to 25 wt. % of a solvent for the polyolefin.
- solvent content is here and hereinafter each time understood to be the amount of solvent in percent by weight of the total weight of polyolefin fibres and solvent in the fibre layer.
- solvent-containing shaped articles obtained according to this process have a higher SEA, because the solvent has no anti-ballistic effect per se, and can hence not contribute to the level of protection, while it does raise the areal density and should hence lower the SEA. It is also surprising that solvent-containing fibres result in a better anti-ballistic quality, because it is known that the presence of solvent reduces the fibre's mechanical properties (in particular because of the higher creep rate and the lower tensile strength and modulus of tension) whereas for a higher anti-ballistic quality the best possible mechanical properties are desired.
- UD shaped articles can be chosen to be lower without any risk of the fibre layers delaminating, that is, at the same ILSS (Inter Laminar Shear Strength). This also raises the SEA of the shaped article.
- UD shaped articles are composites of fibres in a matrix in which the fibres in the fibre layers are unidirectionally oriented and at an angle relative to the fibres in neighbouring fibre layers. Because of the presence of solvent, the matrix content can be reduced by between 2 and 20 times the solvent content, by 10, 15 or even more than 20% of the original matrix content.
- the matrix content can for example be lowered from normal values of between approximately 22 and 30 wt. % to less than 20, preferably less than 13 and more preferably even less than 17 wt. %.
- ‘Fibre’ is understood to be a long, thin object such as a monofilament, a multifilament yarn, a tape, staple fibres, staple fibre yarns, etc.
- the fibres may in principle have any randomly chosen cross-sectional shape.
- ‘Fibre layer’ is understood to be a flat structure expanded in two dimensions containing fibres such as, for example, woven fabrics, knitted fabrics, felts, layers of unidirectionally oriented fibres, etc.
- the fibre layers may or may not contain a matrix material.
- the effect of the invention is obtained already with a shaped article consisting of a single layer, but usually a shaped article will be a stack of two or more fibre layers consolidated by means of compression. Examples of shaped articles are plates, whether or not curved, helmets, cuirasses, door panels, etc.
- the shaped articles that can be obtained according to the invention are particularly suitable for use in anti-ballistic applications.
- polyolefins are suitable for use in the process according to the invention. Particularly suitable as polyolefins are homo- and copolymers of polyethylene and polypropylene. In addition, the polyolefins employed may contain small amounts of one or more other polymers, in particular other alkene-1 polymers. Good results are obtained when linear polyethylene (PE) is chosen as the polyolefin.
- PE linear polyethylene
- Linear polyethylene is here understood to be polyethylene with fewer than 1 side-chain per 100 C atoms, preferably with fewer than 1 side-chain per 300 C atoms, which may moreover contain up to 5 mol % of one or more copolymerizable other alkenes such as propylene, butene, pentene, 4-methylpentene or octene.
- the fibre may contain small amounts of the additives usually used for such fibres, such as antioxidants, spinfinish, thermal stabilizers, pigments, etc.
- the fibre is preferably highly oriented.
- ‘highly oriented’ is understood to be a modulus of at least 500 g/den.
- the modulus is at least 800 and more preferably at least 1000 and most preferably at least 1200 g/den.
- the tensile strength is preferably more than 30 g/den.
- the tensile strength (strength) and the modulus of tension (modulus) have been defined and are determined as described in ASTM D885M, using a nominal gauge length of the fibre of 500 mm, a crosshead speed of 50%/min and Instron 2714 clamps. The fibre is twisted at 31 turns per meter before the measurement.
- the modulus is determined as the gradient between 0.3 and 1% strain.
- the modulus and strength are calculated by dividing the measured tensile forces (in cN) by the titre (in dtex), as determined by weighing 10 meters of fibre.
- the polyolefin fibre in particular the polyethylene fibre, preferably has an intrinsic viscosity (IV) of more than 5 dl/g.
- the polyolefin fibres are highly oriented polyethylene fibres having an intrinsic viscosity of at least 5 dl/g and a modulus of tension of at least 800 g/den. Because of their long molecule chains, polyolefin fibres having such an IV have very good mechanical properties such as a high tensile strength, modulus and energy absorption at break. That is also why the polyolefin is even more preferably a polyethylene having an IV of more than 10 dl/g.
- the IV is determined according to instruction PTC-179 (Hercules Inc. Rev. Apr. 29, 1982) at 135° C. in decalin with the dissolution, time being 15 hours, the anti-oxidant being DBPC in an amount of 2 gr/l of solution and the viscosity at different concentrations being extrapolated to zero concentration.
- the fibre according to the invention also has a fineness of less than 5 denier, more preferably less than 3 denier per filament. It has invention also has a fineness of less than 5 denier, been found that the ballistic properties of such fibres are better.
- the solvent may be on and/or in the fibres and may have been added to the fibre layer in different ways. It may have been applied co the fibre by bringing fibres that are essentially free of solvent, as described above, into contact with the solvent, for example by spraying, dipping or licking. This may be done before or after the fibres that are essentially free of solvent have been formed into a fibre layer.
- the fibres are preferably brought into contact with a mixture of the solvent and a thinning agent, the thinning agent being removed after application to the fibres.
- the advantage of this is a more homogeneous distribution.
- the thinning agent is for example a volatile substance which can easily be removed through evaporation after distribution.
- the solvent has been introduced into the fibre layers as a result of the fibre layers containing solvent-containing polyolefin fibres with a solvent content of 0.02-25 wt. %.
- One of the advantages of the solvent being in the fibre is that the process is less contaminated by the rubbing off of the solvent present on the fibres and, more important, that a comparable anti-ballistic quality can be obtained at a lower solvent content. In this embodiment, very good anti-ballistic results are achieved already at solvent contents of 0.02-5 wt. %.
- Solvent-containing fibres can be produced by bringing the fibre into contact with solvent and allowing the solvent to penetrate the fibre.
- the drawback of this is that several process steps are necessary and that adhering solvent would have to be removed to prevent contamination.
- such fibres are preferably produced directly by spinning a solution of polyolefin and solvent to form filaments and drawing them to a highly oriented state without entirely removing the solvent employed from the fibre (as described in an application by the same applicant that has not yet been disclosed).
- the solvent has been introduced into the fibre layers as a result of the fibre layers containing solvent-containing highly oriented polyolefin fibres with an intrinsic viscosity of at least 5 dl/g, a tensile strength of at least 30 g/den, a modulus of tension of at least 800 g/den and containing 0.05-25 wt. % of a solvent for the polyolefin (relative to the total weight of the fibre), which have been produced by spinning a solution of polyolefin and solvent to form filaments and drawing them to a highly oriented state without completely removing the solvent employed from the fibre.
- solvent is here and hereinafter understood to be a substance that is capable of dissolving the polyolefin concerned.
- Suitable solvents for polyolefins are known to a person skilled in the art. They can for example be chosen from the ‘Polymer Handbook’ by J. Brandrup and E. H. Immergut, third edition, chapter VII, pages 379-402.
- a solvent with the polyolefin employed, in particular polyethylene having a chi-parameter of less than 0.5, more preferably less than 0.45, even more preferably less than 0.4 and most preferably less than 0.35. Chi-parameters of solvents are given in the Handbook of sol.
- suitable solvents for polyolefin, in particular polyethylene are, separately or combined with one another: decalin, tetralin, toluene, lower n-alkanes such as hexane, (para-)xylene, paraffin oil, squalane, mineral oil, paraffin wax, cyclooctane.
- decalin is used and most preferably paraffin oil.
- the fibres contain 0.02-25 wt. % of a solvent for polyolefin before compression. Solvent contents of less than 0.02 wt. % have no, or virtually no, effect. Contents of more than 25 wt. % present the drawback that they generally no longer contribute towards the improvement of, or even detract from, the anti-ballistic properties.
- the SEA increases in accordance with the solvent content up to a certain optimum solvent content, at which the contribution to the energy absorption no longer counterbalances the increase in areal density and the SEA decreases.
- the solvent content is preferably chosen to be optimum in the light of the anti-ballistic quality of the shaped article.
- the optimum solvent content depends on, for example, the fibre configuration, the quality of the solvent chosen and the compression, conditions. For example, to achieve the same improvement in the anti-ballistic properties the amount needed of a very good solvent such as paraffin or decalin will be lower than that needed of a lower-quality solvent and the optimum amount of solvent will be higher at a lower pressure than at a high pressure.
- the solvent content is preferably somewhat higher, of the order of more than 0.5, preferably more than 1 and even more preferably more than 1.5 wt. %.
- the solvent content is preferably more than 1 wt. %, more preferably more than 1.5 wt. %, most preferably more than 2 wt. % and most preferably even more than 3 wt. %.
- a person skilled in the art can readily determine the optimum amount for each condition.
- the fibre layers contain unidirectional solvent-containing highly oriented polyethylene fibres and the solvent has a chi-parameter of less than 0.5
- good anti-ballistic properties are obtained already at relatively low solvent contents of between 0.05 and 5 wt. %.
- the solvent content of the fibre layers is 0.1-2 wt. %, more preferably 0.1-1.5 wt. %, even more preferably 0.1-1.2 wt. % and most preferably 0.05-1 wt. % of the solvent.
- the aforementioned preferences are all with a view to obtaining the highest possible SEA.
- all the fibre layers in the shaped article are essentially the same, so that the aforementioned solvent contents relate to the entire shaped article.
- the solvent content in the process according to the invention is chosen through the choice of the amount added.
- the solvent content of the fibres, fibre layers or shaped articles can be determined in a known way, for example directly by means of infrared techniques or C13 NMR, or indirectly by removing solvent, for example by means of extraction or head-space chromatography or combinations of said techniques.
- the solvent is a volatile solvent.
- the volatile solvent may remain in the shaped article.
- a higher SEA can consequently be achieved.
- the residual volatile solvent content in the shaped article thus obtained is ultimately less than 2%, more preferably at most 1.5% and most preferably at most 1% because there will then be less risk of plastic yield, blistering, delamination, stench, etc.
- the solvent is a non-volatile solvent.
- the advantage of this in comparison with volatile solvents is that there is less risk of blistering and that the shaped article has a better stability, as a result of which the anti-ballistic quality of the shaped articles obtained will also remain at a high level for a longer time.
- Another advantage is that the shaped article does not smell so bad and is not toxic or a health hazard, which is relevant in particular in the case of protection of the body.
- a non-volatile solvent is understood to be a solvent that does virtually not evaporate at a temperature below the polyolefin's melting temperature. Preferably, they are solvents with a boiling temperature that is substantially, preferably 50 to 100 degrees, higher than the fibre's melting temperature. Most preferably, the solvent is a non-volatile paraffin.
- the advantage is that a non-volatile paraffin, in particular a paraffin oil (or mineral oil), is a relatively good solvent having the aforementioned advantages, with minimum risk of reduced stability of the shaped article.
- the solvent may also be a mixture of one or more suitable solvents.
- the solvent is a mixture of a non-volatile solvent, preferably paraffin, and a volatile solvent, the concentration of the volatile solvent in the shaped article formed being at most 2%, more preferably at most 1.5% and most preferably at most 1% (relative to the total fibre weight).
- the mixture has the advantage of a better solvent quality than of the non-volatile solvent component and a good stability.
- the highest possible pressures are preferably used, as for example described in WO97/00766.
- the reported pressures vary from 10 to 165 bar.
- the compression temperature is chosen to be high, but not so high as to cause the ballistic properties to decrease again as a result of softening or melting of the fibres.
- WO97/00766 describes a compression temperature for polyethylene fibres of between 110 and 130° C. As a rule, 125° C. was taken as a safe upper limit. Surprisingly it was found that the best results are obtained precisely at even higher temperatures combined with even higher pressures, in the presence of a solvent in the fibre layers.
- the solvent content is preferably 0.05-5 wt.
- the compression temperature is, with increasing preference, higher than 130, 135, 140, 145 or even 150 degrees, combined with pressures, with increasing preference, higher than 175, 200, 250, 275 or even 300 bar.
- the highest results were obtained at 150° C. and 300 bar, in the presence of 0.05 to 2 wt. % decalin or paraffin.
- UD composites produced according to the process have very good ballistic properties, of up to 145 J/m 2 /kg and higher.
- the invention also relates to a shaped article obtainable according to the process according to the invention described above.
- the invention relates to a shaped article containing one or more fibre layers compressed on top of one another, which contain polyolefin fibres and 0.5 to 25 wt. % of a solvent for the polyolefin.
- Preferred embodiments for the anti-ballistic shaped article follow directly from, and have hence also been described in, the preferred embodiments of the process described above.
- the shaped articles according to the invention have a higher level of protection (at the same areal density) than the known shaped articles.
- the SEA of the shaped article on impact of an AK47 MSC point is at least 115 J/kg/m 2 , preferably more than 120 J/kg/m 2 and even more preferably more than 135 J/kg/m 2 and most preferably more than 145 J/kg/m 2 .
- the best embodiment is a shaped article containing one or more fibre layers compressed on top of one another containing highly oriented polyethylene fibres and at most 30 wt. % of a matrix material (relative to the total weight of the fibre layer), the fibres in the fibre layers being unidirectionally oriented and at an angle with respect to the fibres in neighbouring fibre layers, which fibres have an intrinsic viscosity of at least 5 dl/g, a modulus of tension of at least 300 g/den, a fineness of less than 5 denier per filament and contain 0.05 to 5 wt. % of a non-volatile solvent, which shaped article has a specific energy absorption upon impact of an AK47 MSC point of at least 115 J/kg/m 2 .
- the invention also relates to the use of the shaped article according to the invention in anti-ballistic applications such as helmets, door panels, floor, chair and door armours in cars, tanks, fighter helicopters, etc., insert plates for bullet-proof vests, etc.
- SK76 Dyneema yarn without paraffin was woven into a simple fabric with 8 yarns/cm in the warp and the weft.
- the areal density of the woven fabric was 318 gr/m 2 .
- Twenty layers of this fabric were compressed to form flat panels with 60 micron Stamylex (LLDPE) film between each layer.
- the pressure was 10 bar, the temperature was 125° C. and the compression time was 20 min. After this compression time the panels were cooled while the pressure was maintained.
- the V50 was determined according to the Stanag 2920 standard test using 17 grain FSP.
- the V50 was 532 m/s, corresponding to an energy absorption (SEA) of 21.4 j/kg/m 2 .
- SEA energy absorption
- the properties of the SK76 yarn employed are:
- SK76 Dyneema yarn with a particular paraffin content was produced by means of gel-spinning, under the conditions usually used for SK76, from a solvent to which a particular amount of paraffin had been added.
- Dünmannig paraffin from Merck having a dynamic viscosity of 25-80 MPa/.sec and a density of 0.818-0.875 gr/cm 3 was used as the paraffin.
- the specified paraffin content was calculated on the basis of the percentage of paraffin added to the solvent at complete retention of the paraffin in the fibre during the fibre production process.
- a panel was produced and tested according to Comparative Experiment A, except that SK76 yarns containing approximately 0.8% paraffin solvent were used. The strength and modulus of the yarn were the same as those of the solvent-free yarn. The areal density of the woven fabric was 302 g/m 2 . The resulting V50 of the solvent-containing panel was 560 m/s, corresponding to an energy absorption of 24 J/kg/m 2 .
- Doubled Dyneema SK75 yarns without solvent were woven to form a twill 3/1 style fabric with 3.75 yarns/cm in the warp and weft and an AD of 276 g/m 2 .
- 22 layers of this fabric were compressed with 30-micron Stamylex (LLDPE) film between the layers to form panels and tested in a manner as described in Example 1.
- the V50 was 534 m/s, corresponding to an SEA of 23.8 J/kg/m 2 .
- a twill woven fabric as in Comparative Experiment B was produced, only now using SK75 fibres containing approximately 2000 ppm decalin, as determined with the aid of head-space chromatography. Although the yarn properties were the same, the V50 of the panels was higher, namely 600 m/s, corresponding to an SEA of 28 J/kg/m 2 .
- Four monolayers were formed into a UD stack in which the fibre direction in each monolayer was at an angle of 90 degrees with respect to the fibre direction in the neighbouring layer.
- 75 of such UD stacks were compressed to form an anti-ballistic shaped article at a temperature of 125 degrees Celsius and a pressure of 165 bar for 35 minutes.
- the shaped article was cooled with water while the pressure was maintained.
- the shaped articles were tested according to the Stanag 2920 standard using AK47 MSC rounds. The yarn properties had not been affected by the addition of the paraffin.
- a UD composite was produced and tested according to Examples 3-7, with an AD of 19 kg/m 2 , with 0.8 wt. % paraffin oil and compressed at a pressure of 300 bar at a compression temperature of 150° C. The results are given in the above table.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Composite Materials (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Textile Engineering (AREA)
- Aiming, Guidance, Guns With A Light Source, Armor, Camouflage, And Targets (AREA)
- Artificial Filaments (AREA)
- Nonwoven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
- Strength: 36.0 cN/dtex
- Modulus: 1180 cN/dtex
The strength and the modulus were determined using a Zwick tensile tester, with Instron 2714 clamps, a clamping length of 500 mm and a test drawing rate of 250 mm/min. The modulus was determined between 0.3 and 1%.
Woven Fabric: Example 1
- Strength: 35,1 cN/dtex
- Modulus: 1130 cN/dtex
Twill Woven Fabric: Example 2
fibre | Paraffin (%) | V50 (m/s) | ||
C | SK75 | 0 | <710 | ||
3 | SK75 | 0.4 | 730 | ||
4 | SK75 | 0.8 | 780 | ||
5 | SK76 | 0.4 | 750 | ||
6 | SK76 | 0.8 | 780 | ||
7 | SK76 | 1.2 | 810 | ||
8 | SK76 | 0.8 | 820 | ||
UD Composite: Example 8
Claims (12)
Priority Applications (1)
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US11/936,707 US7811498B2 (en) | 1998-10-26 | 2007-11-07 | Process for the production of a shaped article |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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NL1010399 | 1998-10-26 | ||
NL1010399A NL1010399C1 (en) | 1998-10-26 | 1998-10-26 | Method for manufacturing a molded part. |
PCT/NL1999/000097 WO2000024811A1 (en) | 1998-10-26 | 1999-02-24 | Process for the production of a shaped article |
US09/842,373 US7311963B2 (en) | 1998-10-26 | 2001-04-26 | Process for the production of a shaped article |
US11/936,707 US7811498B2 (en) | 1998-10-26 | 2007-11-07 | Process for the production of a shaped article |
Related Parent Applications (1)
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US09/842,373 Division US7311963B2 (en) | 1998-10-26 | 2001-04-26 | Process for the production of a shaped article |
Publications (2)
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US20080237923A1 US20080237923A1 (en) | 2008-10-02 |
US7811498B2 true US7811498B2 (en) | 2010-10-12 |
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US09/842,373 Expired - Fee Related US7311963B2 (en) | 1998-10-26 | 2001-04-26 | Process for the production of a shaped article |
US11/936,707 Expired - Fee Related US7811498B2 (en) | 1998-10-26 | 2007-11-07 | Process for the production of a shaped article |
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US09/842,373 Expired - Fee Related US7311963B2 (en) | 1998-10-26 | 2001-04-26 | Process for the production of a shaped article |
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US (2) | US7311963B2 (en) |
EP (1) | EP1124885B1 (en) |
CN (1) | CN1203113C (en) |
AU (1) | AU2748799A (en) |
CA (1) | CA2347673C (en) |
DE (1) | DE69907496T2 (en) |
ES (1) | ES2199556T3 (en) |
HK (1) | HK1042104A1 (en) |
IL (1) | IL142793A (en) |
NL (1) | NL1010399C1 (en) |
TW (1) | TW460378B (en) |
WO (1) | WO2000024811A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL1010413C1 (en) † | 1998-10-28 | 2000-05-01 | Dsm Nv | Highly oriented polyolefin fiber. |
GB0128405D0 (en) * | 2001-11-27 | 2002-01-16 | Btg Int Ltd | Process for fabricating polyolefin sheet |
HUE049943T2 (en) | 2003-05-22 | 2020-11-30 | Canco Hungary Invest Ltd | Polymeric articles |
AU2003304692B2 (en) * | 2004-01-01 | 2010-05-27 | Dsm Ip Assets B.V. | Ballistic-resistant article |
EP1647615A1 (en) | 2004-10-14 | 2006-04-19 | DSM IP Assets B.V. | Process for making a monofilament-like product |
EP1647616A1 (en) * | 2004-10-14 | 2006-04-19 | DSM IP Assets B.V. | Process for making a monofilament-like product |
CA2629306A1 (en) | 2005-11-23 | 2007-05-31 | Genentech, Inc. | Methods and compositions related to b cell assays |
EP1993814B1 (en) * | 2006-03-21 | 2011-05-11 | DSM IP Assets B.V. | Process for the manufacture of a shaped part and shaped part obtainable with said process |
KR20110003367A (en) | 2008-04-14 | 2011-01-11 | 다우 코닝 코포레이션 | Emulsions of boron crosslinked organopolysiloxanes |
CN102037088B (en) * | 2008-04-14 | 2014-08-06 | 陶氏康宁公司 | Emulsions of dilatant organopolysiloxanes |
DE102009034514A1 (en) | 2009-07-24 | 2011-02-03 | Lippmann German Ropes Gmbh & Co. Kg | Rope e.g. forest rope, is formed of yarns of polyethylene fiber and outer layer of polyurethane, where core at outer surface is not fused or fused only to extent that ultimate tensile strength of rope exhibits predetermined value |
US8697220B2 (en) | 2009-08-11 | 2014-04-15 | Honeywell International, Inc. | High strength tape articles from ultra-high molecular weight polyethylene |
US8236119B2 (en) | 2009-08-11 | 2012-08-07 | Honeywell International Inc. | High strength ultra-high molecular weight polyethylene tape articles |
FR3007230B1 (en) * | 2013-06-17 | 2015-07-31 | Sdmo Ind | COMMUNICATION METHOD IN A NETWORK INTERCONNECTING AT LEAST TWO GENERATING GROUPS, AND CORRESPONDING INTERFACING DEVICE. |
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- 1999-02-24 CN CNB998150908A patent/CN1203113C/en not_active Expired - Lifetime
- 1999-02-24 CA CA002347673A patent/CA2347673C/en not_active Expired - Lifetime
- 1999-02-24 WO PCT/NL1999/000097 patent/WO2000024811A1/en active IP Right Grant
- 1999-02-24 AU AU27487/99A patent/AU2748799A/en not_active Abandoned
- 1999-02-24 ES ES99907958T patent/ES2199556T3/en not_active Expired - Lifetime
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Also Published As
Publication number | Publication date |
---|---|
WO2000024811A1 (en) | 2000-05-04 |
DE69907496D1 (en) | 2003-06-05 |
CA2347673C (en) | 2009-01-27 |
CA2347673A1 (en) | 2000-05-04 |
IL142793A (en) | 2005-12-18 |
CN1203113C (en) | 2005-05-25 |
TW460378B (en) | 2001-10-21 |
DE69907496T2 (en) | 2004-04-08 |
EP1124885A1 (en) | 2001-08-22 |
CN1332768A (en) | 2002-01-23 |
HK1042104A1 (en) | 2002-08-02 |
IL142793A0 (en) | 2002-03-10 |
NL1010399C1 (en) | 2000-04-27 |
AU2748799A (en) | 2000-05-15 |
US20020001693A1 (en) | 2002-01-03 |
US20080237923A1 (en) | 2008-10-02 |
ES2199556T3 (en) | 2004-02-16 |
EP1124885B1 (en) | 2003-05-02 |
US7311963B2 (en) | 2007-12-25 |
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